Microfluidic platform for integrated plasmonic detection in laminal flow

被引:5
|
作者
Campu, Andreea [1 ,2 ]
Lerouge, Frederic [3 ]
Craciun, Ana-Maria [1 ]
Murariu, Teodora [4 ]
Turcu, Ioan [4 ]
Astilean, Simion [1 ,2 ]
Monica, Focsan [1 ]
机构
[1] Babes Bolyai Univ, Nanobiophoton & Laser Microspectroscopy Ctr, Interdisciplinary Res Inst Bionanosci, Treboniu Laurean 42, Cluj Napoca 400271, Romania
[2] Babes Bolyai Univ, Biomol Phys Dept, Fac Phys, M Kogalniceanu 1, Cluj Napoca 400084, Cluj, Romania
[3] Univ Lyon 1, Ecole Normale Super Lyon, CNRS, UMR 5182,Lab Chim, 46 Allee Italie, F-69364 Lyon 07, France
[4] Natl Inst Res & Dev Isotop & Mol Technol, Donat 67-103, Cluj Napoca 400293, Romania
关键词
microfluidic chip; gold bipyramids; detection in laminal flow; LSPR; SERS; ENHANCED RAMAN-SCATTERING; GOLD NANOBIPYRAMIDS; SURFACE; IMMUNOASSAY; RESONANCE; SERS;
D O I
10.1088/1361-6528/ab8e72
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this work, we propose a novel approach to design robust microfluidic devices with integrated plasmonic transducers allowing portability, reduced analysis time through dynamic measurements and high sensitivity. Specifically, the strategy we apply involves two steps: (i) the controlled deposition of gold bipyramidal nanoparticles (AuBPs) onto a functionalized solid glass substrate and (ii) the integration of the as-fabricated plasmonic substrate into a polydimethylsiloxane (PDMS) microfluidic circuit. The localized surface plasmon resonance (LSPR) sensitivity of the plasmonic-microfluidic device was evaluated by monitoring the optical responses at refractive index changes, proving a bulk sensitivity of 243 nm RIU-1 for the longitudinal LSPR band of isolated AuBPs and 150 nm RIU-1 for the band assigned to end-to-end linked nanoparticles. A strong electric field generated in the gaps between AuBPs-due to the generation of the so-called extrinsic 'hot-spots'-was subsequently proved by the volumetric surface enhanced Raman scattering (SERS) detection of molecules in continuous flow conditions by loading the analyte into the microfluidic channel via a syringe pump. In conclusion, our miniaturized portable microfluidic system aims to detect and identify, in real-time with high accuracy, analyte molecules in laminal flow, thus providing a groundwork for further complex biosensing applications.
引用
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页数:9
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